EP0242968A1 - Borure-oxyde-nitrure de silicium fritté par réaction pour outils de coupe céramiques - Google Patents
Borure-oxyde-nitrure de silicium fritté par réaction pour outils de coupe céramiques Download PDFInfo
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- EP0242968A1 EP0242968A1 EP87302159A EP87302159A EP0242968A1 EP 0242968 A1 EP0242968 A1 EP 0242968A1 EP 87302159 A EP87302159 A EP 87302159A EP 87302159 A EP87302159 A EP 87302159A EP 0242968 A1 EP0242968 A1 EP 0242968A1
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- Prior art keywords
- silicon nitride
- phases
- oxide
- elements
- boride
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- 229910052581 Si3N4 Inorganic materials 0.000 title claims abstract description 47
- 239000000919 ceramic Substances 0.000 title claims abstract description 41
- 238000006243 chemical reaction Methods 0.000 title claims description 18
- 238000005520 cutting process Methods 0.000 title abstract description 25
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims abstract description 24
- 239000000203 mixture Substances 0.000 claims description 47
- 239000000376 reactant Substances 0.000 claims description 20
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 16
- 230000008569 process Effects 0.000 claims description 14
- 229910052768 actinide Inorganic materials 0.000 claims description 12
- 150000001255 actinides Chemical class 0.000 claims description 12
- 229910052747 lanthanoid Inorganic materials 0.000 claims description 12
- 150000002602 lanthanoids Chemical class 0.000 claims description 12
- QYEXBYZXHDUPRC-UHFFFAOYSA-N B#[Ti]#B Chemical compound B#[Ti]#B QYEXBYZXHDUPRC-UHFFFAOYSA-N 0.000 claims description 10
- 229910033181 TiB2 Inorganic materials 0.000 claims description 10
- 239000006104 solid solution Substances 0.000 claims description 10
- 238000010438 heat treatment Methods 0.000 claims description 8
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 8
- 239000002245 particle Substances 0.000 claims description 6
- 238000005245 sintering Methods 0.000 claims description 6
- 230000000737 periodic effect Effects 0.000 claims description 4
- 238000007493 shaping process Methods 0.000 claims description 4
- 229910045601 alloy Inorganic materials 0.000 claims description 2
- 239000000956 alloy Substances 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 229910000765 intermetallic Inorganic materials 0.000 claims description 2
- 229940000425 combination drug Drugs 0.000 claims 1
- 238000003801 milling Methods 0.000 abstract description 19
- 239000000463 material Substances 0.000 abstract description 18
- 229910010293 ceramic material Inorganic materials 0.000 abstract description 5
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 229910052593 corundum Inorganic materials 0.000 description 14
- 229910001845 yogo sapphire Inorganic materials 0.000 description 14
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
- 235000013339 cereals Nutrition 0.000 description 8
- 239000000843 powder Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 230000035939 shock Effects 0.000 description 7
- 238000007731 hot pressing Methods 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 229910052718 tin Inorganic materials 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 230000009977 dual effect Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 230000037361 pathway Effects 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- -1 rare earth metal carbides Chemical class 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Chemical group [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 description 2
- 229910000615 4150 steel Inorganic materials 0.000 description 1
- 229910003564 SiAlON Inorganic materials 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229910034327 TiC Inorganic materials 0.000 description 1
- 229910007948 ZrB2 Inorganic materials 0.000 description 1
- CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 description 1
- OJMOMXZKOWKUTA-UHFFFAOYSA-N aluminum;borate Chemical class [Al+3].[O-]B([O-])[O-] OJMOMXZKOWKUTA-UHFFFAOYSA-N 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- VWZIXVXBCBBRGP-UHFFFAOYSA-N boron;zirconium Chemical compound B#[Zr]#B VWZIXVXBCBBRGP-UHFFFAOYSA-N 0.000 description 1
- 238000004814 ceramic processing Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 235000011868 grain product Nutrition 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000003966 growth inhibitor Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 229910052863 mullite Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
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Definitions
- This invention relates to reaction sintered boride-oxide-silicon nitride for ceramic cutting tools.
- the field of the invention is oxide-boride-silicon nitride ceramics where addition of silicon nitride to the boride/oxide phases eliminates cracking during formation of the body and increases wear resistance ad impact shock resistance for use as a durable wear material, interfacing material and as a cutting tool insert.
- cutting tool inserts were fashioned from metals. As higher speeds of cutting (>500 surface feet per minute, (sfm)) were achieved, metals proved less than satisfactory due to their tendency to chemically react with the workpiece. Nitride, carbide, and oxide coatings were applied to cutting tool metal inserts, however, this improvement is a function of the integrity of the metal coating and eventually wears to the metal substrate.
- cutting tool inserts are function and/or workpiece specific. Inserts for turning are not used as milling inserts and vice versa.
- the technologies have tended toward dichotomization with ceramic turning tool insert compositions varying significantly from milling tool insert compositions.
- the ceramic tool milling inserts have been based in the Si3N4 technology while ceramic tool turning inserts have been based in the Al2O3 technology.
- the marriage of these technologies produces a ceramic tool insert which exhibits surprising durability characteristics for use as either a turning or milling tool insert.
- U.S. Patent 4,204,873 discloses the addition of WC and TiN to the Al2O3 sintered ceramic body.
- U.S. Patent 4,366,354 discloses the addition of ZrO2, TiN or TiC, and rare earth metal carbides to the Al2O3 ceramic body.
- U.S. Patent 4,543,343 discloses addition of TiB2 and ZrO2 to the Al2O3 ceramic body.
- Typical ceramic milling tool inserts are a Si3N4 sintered ceramic body modified with various metal oxides.
- U.S. Patent 4,434,238 discloses a Si3N4 body modified with SiO2 and Y2O3.
- U.S. Patent 4,264,548 discloses a Si3N4 body modified with SiO2, Y2O3, and Al2O3.
- the turning test looks to durability and is a function of the cutting speed measured in surface feet per minute (sfm). Typically, cutting speeds for the industry average 500 sfm.
- the milling test looks to the toughness of the material and is measured by the number of cuts as a function of flank wear.
- the advantage of ceramic inserts is their durability and availability of use at much higher surface feet per minute, an order of magnitude larger. The disadvantage has been low reliability since ceramic materials have tended to chip due to insert tip fracture.
- the invention utilizes, but is not limited to, the process known as Exchange Reaction Hot Pressing (ERHP) as disclosed in European patent application publication No. 0115689 issued August 15, 1984. It is previously known that diluents, modifiers, and fillers could be added to the ERHP reactions.
- ERHP Exchange Reaction Hot Pressing
- the novel discovery is that addition of silicon nitride to the oxide-boride phases helps to eliminate cracking during formation of the body and increases wear and impact shock resistance of cutting tool insert material which yields a cutting tool insert with superior performance.
- the invention is a ceramic body which is characterized by uniformly fine-grained and intimately interdispersed phases of oxides, borides, silicon nitrides, and/or silicon-aluminum oxynitrides. Furthermore, the invention is a ceramic composition consisting essentially of a dense homogeneous sintered body whose composition is selected from (a) composition A consisting essentially of on a mole per cent basis, 2 to 80% silicon nitride, where some or all of the silicon nitride is present as a separate phase or in solid solution with aluminum oxide as silicon-aluminum-oxynitride and about 10 to 90% boride phase or phases of one or more of the elements of groups 3b including lanthanide and actinide series elements, 4b, 5b, 6b, and 25 to 88% oxide phases or phases of one or more of the elements of groups 3a, 4a, 3b including lanthanide and actinide series elements, 4b, 5b, 6b and 8 of the periodic table; and
- reaction hot pressed body of this invention is noted for virtual absence of open porosity, toughness, and hardness for wear resistance, elimination of cracking during body formation, and impact shock resistance. It is also notable that these valuable properties can be attained by heating the mixture of reactants to temperature not greater than about 1600°C and without need for any grain growth inhibitor or sintering aid.
- An advantageous form of the invention is a reaction sintered oxide-boride-silicon nitride ceramic body consisting essentially of a fine-grained, homogeneous, intimate interdispersion of:
- Reaction sintering involves the dual effects of reaction between and sintering together of the admixed reactants at temperature causing the reaction to occur and be substantially completed. It is to be understood that the reaction as in the ERHP process proceeds stepwise, the reactants forming products which then automatically sinter. It may be effected at atmospheric, subatmospheric, or superatmospheric pressure. The latter condition involves the substantially simultaneous shaping and heating steps of hot pressing to produce a body of the invention with very little or no open porosity and highest strength properties, although some preliminary separate pressing or heating of the reactant admixture may be advantageously done. Where open porosity is desired in an otherwise tough and hard body of the invention, the separate heating step at atmospheric or subatmospheric pressure may be employed sequentially following the shaping step.
- a unique advantage of the ERHP process is that fine grained ceramic materials are produced independent of the particle size of the reactant powders.
- the grain sizes of the grains in the reacted body are not dependent on and are generally much smaller than the particles of the reacting powder.
- the maximum grain size of any product phase should not be substantially greater than 15 ⁇ m and preferably not substantially greater than 5 ⁇ m.
- This fine grain microstructure contributes significantly to the excellent mechanical and physical properties of the ERHP materials.
- a body formed by conventional ceramic processing requires smaller reactant particle grain sizes to achieve comparable ERHP product grain sizes. Generally, grain growth is exhibited during and is a result of the sintering process. Therefore, to achieve small grain products, smaller grained reactants are required.
- the body of the invention may contain, as part of the boride, oxide, and/or silicon nitride phases, diluent which is a nonreacted portion of the reactant admixture as a stoichiometric excess amount of a reactant and/or as a boride or oxide according to the aforesaid invention definition but different from the reactants.
- Silicon nitride does not "react” as do the other batch reactants but does go into solid solution with the aluminum oxide or remains as a separate phase.
- This solid solution can consist of one or more phases of that class of materials known as silicon-aluminum-oxynitrides (SiAlONs).
- the element forming the boride cation is different than the element forming the oxide cation.
- Nonreacting phases such as aluminum oxide, can be added to the reactants as nonreacting filler materials.
- cutting tools of the present invention may be formed by hot pressing in accordance with conventional techniques.
- These ceramic compositions provide excellent wear resistance with commercially acceptable toughness. Significantly these compositions perform well in both the wear and shock tests indicating their broad applicability as reliable ceramic tool inserts for both turning and milling operations.
- the compositions presented offer the bifunctional role, the ERHP process which is the preferred method of making these compositions provides a relatively easy pathway to an end product which can be finished to the required size and shape.
- the present invention provides long lived materials which are functional in both tool insert operations and provide the operator with a range of working speeds and work piece cutting depths that heretofore, ceramic materials have been unable to achieve.
- Speeds ranging from a low of 500 sfm to a high of 5000 sfm may be utilized with the current compositions. These compositions have also shown superior cutting performance for hard and soft steels and cast iron.
- Table 1 Shown in Table 1 are the ceramic compositions tested as inserts.
- compositions tested were as follows: TiB2 ranged from 13 to 95 wt. %, in combination with or exclusive of Al2O3 which ranged from 0 to 83 wt. %, and in combination with Si3N4 which ranged from 4 to 75 wt. %.
- Hardness is estimated on the Rockwell Hardness scale. Table 2 shows representative values of the range of measured properties. Typically densities on the order of 3.4 g/cm3 have been reported and Rockwell Hardness values ranging from 87 to 91 for Si3N4 containing ceramic insert tools. Densities for the current compositions range from 3.28 to 3.95 g/cm3. Rockwell Hardness A values measured in the range of 90.6 to 94.2. All samples evidence very low open porosity. The product material should have a maximum open porosity substantially not greater than 5% and a preferred open porosity substantially not greater than 2%.
- Bodies comprising essentially boride/oxide/silicon nitride are produced by adding silicon nitride powder to the reactant powder mixture used to make the boride/oxide phases.
- silicon nitride powder For example, the following powders were intimately mixed in the appropriate proportions: Si3N4 + TiO2 + AlB12 + Al by suitable means such as vibromilling.
- the mixed powder is then charged to a graphite mold and heated under pressure (hot pressed) to a temperature sufficient to cause the exothermic reaction of the TiO2 + AlB12 + Al wherein the formation and densification of the final product phases occur.
- the resulting body consists of the following phases: TiB2, Al2O3, Si3N4 (alpha and beta), SiAlON phases, and may contain trace amounts ( ⁇ 5 wt. %) of TiN, unreacted reactants, silicates, nitrogen mullite, silicon, and aluminum borates.
- the phases formed are a function of the purity of the reactants, the processing temperature, the amount of Si3N4 added and the amount and kind of diluents added to the reaction. Silicon nitride does not "react" as do the other batch reactants but does go into solid solution with the aluminum oxide. This solid solution can consist of one or more phases of SiAlONs.
- Sample A was prepared according to the following equation: 35% Si3N4 + 65% (6TiO2 + AlB12 + 7Al) ⁇ 35% Si3N4 + 65 (6TiB2 + 4Al2O3.
- Si3N4 (with a Mean Particle Size (MPS) of 2.1 microns), TiO2 (with an MPS ⁇ 1 micron), AlB12 (with an MPS of 9.4 microns), and Al (with an MPS of 6.4 microns) were mixed in a slurry of isopropanol.
- the slurry was vibromilled using 0.5 inch diameter alumina grinding media for 16 hours.
- the slurry was dried and a portion of the powder hot pressed in a graphite mold in vacuum at a maximum hold temperature of 1600°C and top pressure of 6000 psi. The sample was held at maximum temperature and pressure for 30 minutes.
- compositions were subjected to a turning test under the following conditions: insert geometry: SNG-433, edge preparation: T2, material: 4150 steel, depth of cut: .075 inches, cutting speed 850 sfm, and a lead angle: 15°.
- insert geometry SNG-433
- edge preparation T2
- material 4150 steel
- depth of cut .075 inches
- cutting speed 850 sfm and a lead angle: 15°.
- Table 5 shows the results of the milling test.
- the materials tested were made by the ERHP process and subject to the shock test under the following conditions: cutting speed: 1200 sfm, depth of cut: .075 inches, feed rate: .0025 inches increased by .0025 inches on each 5th cut, edge preparation: T2 and a lead angle of 15°.
- the workpiece was cast iron, 200 BHN.
- Sample X is of a composition not made by the ERHP process but by hot pressing.
- a mixture of 35 wt. % Si3N4, 33 wt. % TiB2, and 32 wt. % Al2O3 was vibromilled in isopropanol using alumina balls for 16 hours. After vibromilling the solvent was evaporated. Part of the powder mixture was hot pressed in a POCO graphite mold applying full pressure of 6000 psi at the start and maintaining the pressure throughout the cycle. The sample was heated at 27°C per minute up to 1600°C and held at temperature for 30 minutes, then cooled at furnace rate. The resulting bulk density was 3.50 g/cm3.
- Combining the results of the turning and milling tests indicates the preferred embodiment of the inventive composition to be useful as a ceramic cutting tool insert for the combinational use as a milling and turning tool insert.
- the preferred combination comprises 10 to 70 mole % TiB2, 1 to 70 mole % Al2O3, and 5 to 55 mole % of Si3N4.
- the data further indicate that the following two compositional ranges for each constituent exhibit preferred compositional combinations comprising mole % as: 10 to 55% and 12 to 35% TiB2, 5 to 50% and 5 to 40% Si3N4, as well as 25 to 70% and 28 to 70% Al2O3.
- These compositional ranges focus on the optimum ranges for use of these combinations as both turning and milling ceramic inserts. As well, these ranges exhibit properties of toughness and hardness which encompass the functional capability for milling and turning which may be applied to a range of workpiece materials.
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- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
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Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85389786A | 1986-04-21 | 1986-04-21 | |
| US853897 | 1986-04-21 | ||
| US88692586A | 1986-07-18 | 1986-07-18 | |
| US886925 | 1986-07-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0242968A1 true EP0242968A1 (fr) | 1987-10-28 |
Family
ID=27127196
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP87302159A Ceased EP0242968A1 (fr) | 1986-04-21 | 1987-03-13 | Borure-oxyde-nitrure de silicium fritté par réaction pour outils de coupe céramiques |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP0242968A1 (fr) |
| KR (1) | KR870009964A (fr) |
| CA (1) | CA1260505A (fr) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6040256A (en) * | 1993-10-12 | 2000-03-21 | Isuzu Ceramics Research Institute Co., Ltd. | Method for producing a reaction sintered ceramic |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0115177A2 (fr) * | 1982-12-30 | 1984-08-08 | Corning Glass Works | Corps céramique polyphasé fritté par réaction |
| EP0115689A2 (fr) * | 1982-12-30 | 1984-08-15 | Corning Glass Works | Corps céramique en oxyde-borure fritté par réaction et son application dans les cellules électrolytiques pour la production de l'aluminium |
-
1987
- 1987-03-06 CA CA000531413A patent/CA1260505A/fr not_active Expired
- 1987-03-13 EP EP87302159A patent/EP0242968A1/fr not_active Ceased
- 1987-04-21 KR KR870003933A patent/KR870009964A/ko not_active Withdrawn
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0115177A2 (fr) * | 1982-12-30 | 1984-08-08 | Corning Glass Works | Corps céramique polyphasé fritté par réaction |
| EP0115689A2 (fr) * | 1982-12-30 | 1984-08-15 | Corning Glass Works | Corps céramique en oxyde-borure fritté par réaction et son application dans les cellules électrolytiques pour la production de l'aluminium |
Non-Patent Citations (2)
| Title |
|---|
| DERWENT ACCESSION No. 86-45 740, Questel Telesystemes (WPIL) DERWENT PUBLICATIONS LTD., London; & JP-A 60 264 368 (MITSUBISHI METAL KK ) * Abstract * * |
| DERWENT ACCESSION No. 86-78 156, Questel Telesystemes (WPIL) DERWENT PUBLICATIONS LTD., London, * ABSTRACT * * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6040256A (en) * | 1993-10-12 | 2000-03-21 | Isuzu Ceramics Research Institute Co., Ltd. | Method for producing a reaction sintered ceramic |
Also Published As
| Publication number | Publication date |
|---|---|
| CA1260505A (fr) | 1989-09-26 |
| KR870009964A (ko) | 1987-11-30 |
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